International product submissions

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Anonymous said:
Can we get more internal B&L people on these international submission projects?
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Nope. You are on your own. No one cares about a product that has already received approval by the FDA. The assumption is that it will approve itself with very little action by the functional groups. What you get is a lot of complaining and very little action by management to staff these projects appropriately or to assign them to a VPs objectives. So they just sit and don't move forward.
 



You are right. No one takes these product submissions seriously. Why does it take so long for products to get approved in foreign countries?

Because so little weight is put on the VP and Director's objectives for these projects. If the VPs and the Directors for each functional group was held accountable maybe there would be some movement in this area.
 






latin american and asia pacific regulatory had an approximately 90% turnover this last year. These registrations are sitting in queue while people are learning their jobs...
 



Anonymous said:
latin american and asia pacific regulatory had an approximately 90% turnover this last year. These registrations are sitting in queue while people are learning their jobs...
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D&R is not helping out either. Not enough resources dedicated to these projects. 90% turnover in two key regions of the world means that B+L is not serious about getting approval. Likely because WP hopes to sell B+L way before the product approval come through.

This just shows what a fluff, fake company B+L is. Good luck with the IPO. It will drop like a rock just like facebook.
 



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